These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 17036309)

  • 1. Parietal bone agenesis with gracile bones and splenic hypoplasia/aplasia: clinico-pathologic report and differential diagnosis with review of cranio-gracile bone syndromes, "osteocraniostenosis" and Kleeblattschädel.
    Spear GS
    Am J Med Genet A; 2006 Nov; 140(21):2341-8. PubMed ID: 17036309
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Osteocraniosplenic Syndrome-Hypomineralized Skull with Gracile Long Bones and Splenic Hypoplasia: A Case Report and Literature Review.
    Puvabanditsin S; February M; Stefano VD; Vinod S; Minerowicz C; Hussein K; Mayne J; Mehta R
    Genet Couns; 2016; 27(2):149-57. PubMed ID: 29485259
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Osteocraniostenosis-hypomineralized skull with gracile long bones and splenic hypoplasia. Four new cases with distinctive chondro-osseous morphology.
    Elliott AM; Wilcox WR; Spear GS; Field FM; Steffensen TS; Friedman BD; Rimoin DL; Lachman RS
    Am J Med Genet A; 2006 Jul; 140(14):1553-63. PubMed ID: 16770805
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Report of a novel variant in the FAM111A gene in a fetus with multiple anomalies including gracile bones, hypoplastic spleen, and hypomineralized skull.
    Müller R; Steffensen T; Krstić N; Cain MA
    Am J Med Genet A; 2021 Jun; 185(6):1903-1907. PubMed ID: 33750016
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Gracile bones, periostal appositions, hypomineralization of the cranial vault, and mental retardation in brothers: milder variant of osteocraniostenosis or new syndrome?
    Verloes A; Garel C; Robertson S; Le Merrer M; Baumann C
    Am J Med Genet A; 2005 Aug; 137(2):199-203. PubMed ID: 16086393
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Parietal bone agenesis and associated multiple congenital anomalies.
    de Heer IM; van Nesselrooij BP; Spliet W; Vermeij-Keers C
    J Craniofac Surg; 2003 Mar; 14(2):192-6. PubMed ID: 12621289
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Osteocraniostenosis.
    Verloes A; Narcy F; Grattagliano B; Delezoide AL; Guibaud P; Schaaps JP; Le Merrer M; Maroteaux P
    J Med Genet; 1994 Oct; 31(10):772-8. PubMed ID: 7837254
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and Molecular Diagnosis of Osteocraniostenosis in Fetuses and Newborns: Prenatal Ultrasound, Clinical, Radiological and Pathological Features.
    Rosato S; Unger S; Campos-Xavier B; Caraffi SG; Beltrami L; Pollazzon M; Ivanovski I; Castori M; Bonasoni MP; Comitini G; Nikkels PGJ; Lindstrom K; Umandap C; Superti-Furga A; Garavelli L
    Genes (Basel); 2022 Jan; 13(2):. PubMed ID: 35205306
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Craniometadiaphyseal dysplasia, wormian bone type.
    Santolaya JM; Hall CM; García-Miñaur S; Delgado A
    Am J Med Genet; 1998 May; 77(3):241-5. PubMed ID: 9605592
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Gracile bone dysplasias.
    Kozlowski K; Masel J; Sillence DO; Arbuckle S; Juttnerova V
    Pediatr Radiol; 2002 Sep; 32(9):629-34. PubMed ID: 12195301
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Brief clinical report: lethal multiple pterygium syndrome in an 18-week fetus with hydrops.
    Isaacson G; Gargus JJ; Mahoney MJ
    Am J Med Genet; 1984 Apr; 17(4):835-9. PubMed ID: 6720748
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenital bowing of the long bones associated with camptodactyly, talipes equinovarus and agenesis of the corpus callosum.
    Al-Gazali LI; Bakir M; Hamid ZM; Nath R; Haas D
    Clin Dysmorphol; 2000 Apr; 9(2):93-7. PubMed ID: 10826618
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Osteocraniostenosis in a fetus with a 46,XX/46,XY karyotype.
    Brennan P; Hall C
    Clin Dysmorphol; 2002 Jan; 11(1):57-61. PubMed ID: 11822707
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A unique case of congenital bilateral absence of parietal bones in a neonate.
    Dunn R; Stout S; Dix J
    J Forensic Sci; 1991 Mar; 36(2):593-8. PubMed ID: 2066733
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Agenesis of parietal bones with restoration of the cranial vault. Case report.
    Sela M; Sahar A; Lewin-Epstein J
    J Neurosurg; 1979 May; 50(5):674-6. PubMed ID: 430162
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Fryns syndrome: report of the first case in the national literature].
    Rentería-Ibarra M; Frías-Márquez SG; Michel-Aceves RJ; Navarrete-Arellano M
    Bol Med Hosp Infant Mex; 1993 Sep; 50(9):666-70. PubMed ID: 8373549
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Congenital agenesis of cranial bones associated with hydrocephalus: a case report].
    Moscote-Salazar LR; Castellar-Leones SM; Alcalá-Cerra G; Gutiérrez-Paternina JJ
    Bol Asoc Med P R; 2013; 105(1):54-6. PubMed ID: 23767388
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fibrochondrogenesis: clinical and radiological features.
    al-Gazali LI; Bakalinova D; Bakir M; Dawodu A
    Clin Dysmorphol; 1997 Apr; 6(2):157-63. PubMed ID: 9134297
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Congenital absence of the parietal bones in a family].
    Zabek M
    Wiad Lek; 1987 Jan; 40(1):33-8. PubMed ID: 3590786
    [No Abstract]   [Full Text] [Related]  

  • 20. Locking and reverse molding of the fetal skull.
    de la Fuente AA
    Pediatr Pathol; 1991; 11(2):271-80. PubMed ID: 2052509
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.